Results 41 to 50 of about 37,356 (255)
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena +13 more
wiley +1 more source
[Evaluation of the risk of abortion abuse resulting from the two-week legal delay in France]. [PDF]
, 2002 A national consensus on foetal abnormalities to be searched for, and not to be searched for (Number of fingers? Upper lip?...) and the eventual detection of the gender during sonography of the 1st trimester is urgent in view of the technological progress
Alouini, Souhail +4 more
core +2 more sources
Humans are not unique: difficult birth is common in placental mammals
Biological Reviews, EarlyView.ABSTRACT Human childbirth is widely presumed to be uniquely difficult and dangerous compared to birth in other mammals. Tight fetopelvic proportions can result in obstructed labour and contribute to high rates of maternal and neonatal mortality. Ideas summarised under the ‘obstetrical dilemma’ have contributed to this assumption by explaining difficult
Nicole D. S. Grunstra
wiley +1 more source
Doit-on systématiquement pratiquer le massage périnéal pendant la période du prénatal ?: travail de Bachelor [PDF]
, 2015 Introduction : Les lésions périnéales suite à un accouchement peuvent engendrer beaucoup d’impacts néfastes sur la vie quotidienne des femmes. Il a été démontré que ces problèmes sont moins communs chez les femmes ayant un périnée intact suite à un ...
Kopp, Soraya +2 more
core
Une politique de santé "a priori". Le dépistage néonatal de la mucoviscidose en Bretagne
, 2004 Le dépistage néonatal de la mucoviscidose (DNM), qui fait l'objet d'un débat, au plan international, sur son opportunité, a été décidé officiellement en 2002 en France.
Vailly, Joëlle
core +2 more sources
Self‐limited neonatal epilepsy with 2q24.3 duplications: Case series and literature review
Epileptic Disorders, EarlyView.Abstract Objective To clarify the phenotypic spectrum associated with duplications involving the 2q24.3 region, which includes a cluster of genes encoding sodium channel subunits (SCN1A, SCN2A, SCN3A, SCN7A, and SCN9A). Methods We reviewed our research database for patients with epilepsy and 2q24.3 duplication and performed thorough phenotyping.
Saba Al Rawahi, Kenneth A. Myers
wiley +1 more source
BMC Pregnancy and Childbirth, 2019 Background Globally, Gestational Diabetes Mellitus (GDM) is rising, but it is a neglected health threat to mothers and their children in low resource countries.
Achenef Asmamaw Muche +2 more
doaj +1 more source
A Systematic Scoping Review of Factors Contributing to Loss of Control Eating During Pregnancy
European Eating Disorders Review, EarlyView.ABSTRACT Objective Evidence suggests loss of control eating (LOC) during pregnancy is prevalent and linked to adverse health consequences for birthing individuals and their offspring; however, factors underlying risk for prenatal LOC remain unclear.
Riley J. Jouppi +3 more
wiley +1 more source
Cystic lymphangioma of the mesentery [PDF]
, 2010 peer reviewedCystic lymphangioma of the mesentery is a benign condition, probably of malformative origin, and frequently appearing in infancy. Its symptomatology can be very polymorphic.
Belaiche, Jacques +7 more
core
International Journal of Gynecology &Obstetrics, Volume 169, Issue 1, Page 299-309, April 2025.Abstract Objective To investigate whether induction/augmentation of labor in pregnant women with anemia increases the risk of postpartum hemorrhage (PPH) and whether this risk varied by indications for labor induction/augmentation and by anemia severity in pregnancy.
Tuck Seng Cheng +21 more
wiley +1 more source